JP4936893B2 - 基質処理用ポリオルガノシロキサン組成物 - Google Patents
基質処理用ポリオルガノシロキサン組成物 Download PDFInfo
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- JP4936893B2 JP4936893B2 JP2006530191A JP2006530191A JP4936893B2 JP 4936893 B2 JP4936893 B2 JP 4936893B2 JP 2006530191 A JP2006530191 A JP 2006530191A JP 2006530191 A JP2006530191 A JP 2006530191A JP 4936893 B2 JP4936893 B2 JP 4936893B2
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- Prior art keywords
- group
- amino
- ammonium
- groups
- polysiloxane compound
- Prior art date
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- 239000000203 mixture Substances 0.000 title claims abstract description 147
- 239000000758 substrate Substances 0.000 title abstract description 28
- -1 polysiloxanes Polymers 0.000 claims abstract description 193
- 229920001296 polysiloxane Polymers 0.000 claims abstract description 64
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims abstract description 38
- 150000001875 compounds Chemical class 0.000 claims description 65
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 52
- 125000000962 organic group Chemical group 0.000 claims description 41
- 125000004432 carbon atom Chemical group C* 0.000 claims description 33
- 238000000034 method Methods 0.000 claims description 33
- 229910052757 nitrogen Inorganic materials 0.000 claims description 33
- 125000000217 alkyl group Chemical group 0.000 claims description 27
- 229920006395 saturated elastomer Polymers 0.000 claims description 26
- 229910052799 carbon Inorganic materials 0.000 claims description 25
- 125000004122 cyclic group Chemical group 0.000 claims description 25
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 25
- 229920000570 polyether Chemical group 0.000 claims description 23
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 23
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 22
- 239000007788 liquid Substances 0.000 claims description 22
- 239000004721 Polyphenylene oxide Chemical group 0.000 claims description 21
- 229910052710 silicon Inorganic materials 0.000 claims description 21
- 239000004094 surface-active agent Substances 0.000 claims description 21
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 19
- 125000002029 aromatic hydrocarbon group Chemical group 0.000 claims description 17
- 150000001721 carbon Chemical group 0.000 claims description 17
- 239000007787 solid Substances 0.000 claims description 16
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- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 12
- 125000001424 substituent group Chemical group 0.000 claims description 12
- 239000004744 fabric Substances 0.000 claims description 11
- 229910052739 hydrogen Inorganic materials 0.000 claims description 11
- 239000002253 acid Substances 0.000 claims description 10
- 125000000623 heterocyclic group Chemical group 0.000 claims description 10
- 239000001257 hydrogen Substances 0.000 claims description 10
- 150000003839 salts Chemical class 0.000 claims description 10
- 125000005375 organosiloxane group Chemical group 0.000 claims description 8
- 239000012876 carrier material Substances 0.000 claims description 7
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 6
- 239000000470 constituent Substances 0.000 claims description 6
- 239000003960 organic solvent Substances 0.000 claims description 6
- 150000003856 quaternary ammonium compounds Chemical class 0.000 claims description 6
- 239000000969 carrier Substances 0.000 claims description 5
- 125000004663 dialkyl amino group Chemical group 0.000 claims description 5
- NELREAXCVQVNGC-UHFFFAOYSA-N ethynethiolate Chemical group [S]C#[C] NELREAXCVQVNGC-UHFFFAOYSA-N 0.000 claims description 4
- 125000001153 fluoro group Chemical group F* 0.000 claims description 4
- 150000002431 hydrogen Chemical class 0.000 claims description 4
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- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 3
- 125000003282 alkyl amino group Chemical group 0.000 claims description 3
- 239000003139 biocide Substances 0.000 claims description 3
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- 125000004185 ester group Chemical group 0.000 claims description 2
- 238000006386 neutralization reaction Methods 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 abstract description 25
- 239000000123 paper Substances 0.000 description 85
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 26
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- 238000009472 formulation Methods 0.000 description 21
- 230000006870 function Effects 0.000 description 21
- 125000001183 hydrocarbyl group Chemical group 0.000 description 17
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 16
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- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 16
- 239000000194 fatty acid Substances 0.000 description 16
- 150000004665 fatty acids Chemical class 0.000 description 16
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 15
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- 150000002148 esters Chemical class 0.000 description 14
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 13
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- 229930195729 fatty acid Natural products 0.000 description 13
- 239000000463 material Substances 0.000 description 13
- 238000002360 preparation method Methods 0.000 description 13
- 235000002639 sodium chloride Nutrition 0.000 description 13
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 12
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 12
- 150000001412 amines Chemical class 0.000 description 12
- 239000000460 chlorine Substances 0.000 description 12
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 12
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 12
- 238000002156 mixing Methods 0.000 description 11
- 239000000126 substance Substances 0.000 description 11
- 238000012360 testing method Methods 0.000 description 11
- 125000003277 amino group Chemical group 0.000 description 10
- 125000004193 piperazinyl group Chemical group 0.000 description 10
- 229920000642 polymer Polymers 0.000 description 10
- 239000003760 tallow Substances 0.000 description 10
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 9
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 9
- 150000004985 diamines Chemical class 0.000 description 9
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 9
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- 238000005956 quaternization reaction Methods 0.000 description 9
- 150000003254 radicals Chemical class 0.000 description 9
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 8
- 229920001577 copolymer Polymers 0.000 description 8
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 8
- 238000006116 polymerization reaction Methods 0.000 description 8
- 235000000346 sugar Nutrition 0.000 description 8
- 125000001302 tertiary amino group Chemical group 0.000 description 8
- QLAJNZSPVITUCQ-UHFFFAOYSA-N 1,3,2-dioxathietane 2,2-dioxide Chemical compound O=S1(=O)OCO1 QLAJNZSPVITUCQ-UHFFFAOYSA-N 0.000 description 7
- 125000002947 alkylene group Chemical group 0.000 description 7
- 150000001450 anions Chemical class 0.000 description 7
- 230000000052 comparative effect Effects 0.000 description 7
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- 150000002118 epoxides Chemical class 0.000 description 7
- 238000011156 evaluation Methods 0.000 description 7
- 239000012048 reactive intermediate Substances 0.000 description 7
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 6
- 239000000654 additive Substances 0.000 description 6
- 125000003118 aryl group Chemical group 0.000 description 6
- 239000003093 cationic surfactant Substances 0.000 description 6
- 229920002678 cellulose Polymers 0.000 description 6
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 6
- 150000002500 ions Chemical class 0.000 description 6
- 239000002736 nonionic surfactant Substances 0.000 description 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 6
- 230000008569 process Effects 0.000 description 6
- 238000006467 substitution reaction Methods 0.000 description 6
- VDZOOKBUILJEDG-UHFFFAOYSA-M tetrabutylammonium hydroxide Chemical compound [OH-].CCCC[N+](CCCC)(CCCC)CCCC VDZOOKBUILJEDG-UHFFFAOYSA-M 0.000 description 6
- HBXWUCXDUUJDRB-UHFFFAOYSA-N 1-octadecoxyoctadecane Chemical compound CCCCCCCCCCCCCCCCCCOCCCCCCCCCCCCCCCCCC HBXWUCXDUUJDRB-UHFFFAOYSA-N 0.000 description 5
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 5
- 239000005639 Lauric acid Substances 0.000 description 5
- 150000001298 alcohols Chemical class 0.000 description 5
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- 239000003599 detergent Substances 0.000 description 5
- 150000002009 diols Chemical class 0.000 description 5
- 230000002209 hydrophobic effect Effects 0.000 description 5
- 238000006459 hydrosilylation reaction Methods 0.000 description 5
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 5
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 5
- YPFDHNVEDLHUCE-UHFFFAOYSA-N propane-1,3-diol Chemical compound OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 5
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 5
- 238000005507 spraying Methods 0.000 description 5
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- 150000003512 tertiary amines Chemical class 0.000 description 5
- 239000004753 textile Substances 0.000 description 5
- 239000002759 woven fabric Substances 0.000 description 5
- GVNVAWHJIKLAGL-UHFFFAOYSA-N 2-(cyclohexen-1-yl)cyclohexan-1-one Chemical compound O=C1CCCCC1C1=CCCCC1 GVNVAWHJIKLAGL-UHFFFAOYSA-N 0.000 description 4
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 4
- 101150065749 Churc1 gene Proteins 0.000 description 4
- 235000013162 Cocos nucifera Nutrition 0.000 description 4
- 244000060011 Cocos nucifera Species 0.000 description 4
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 4
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 4
- 102100038239 Protein Churchill Human genes 0.000 description 4
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
- 235000021355 Stearic acid Nutrition 0.000 description 4
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 4
- 238000010521 absorption reaction Methods 0.000 description 4
- 150000008051 alkyl sulfates Chemical class 0.000 description 4
- 238000009835 boiling Methods 0.000 description 4
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
- 150000007942 carboxylates Chemical class 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 239000004205 dimethyl polysiloxane Substances 0.000 description 4
- 125000003700 epoxy group Chemical group 0.000 description 4
- 125000000524 functional group Chemical group 0.000 description 4
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 4
- TXXWBTOATXBWDR-UHFFFAOYSA-N n,n,n',n'-tetramethylhexane-1,6-diamine Chemical compound CN(C)CCCCCCN(C)C TXXWBTOATXBWDR-UHFFFAOYSA-N 0.000 description 4
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 4
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- 229910019142 PO4 Inorganic materials 0.000 description 2
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- SBOJXQVPLKSXOG-UHFFFAOYSA-N o-amino-hydroxylamine Chemical group NON SBOJXQVPLKSXOG-UHFFFAOYSA-N 0.000 description 1
- IOQPZZOEVPZRBK-UHFFFAOYSA-N octan-1-amine Chemical compound CCCCCCCCN IOQPZZOEVPZRBK-UHFFFAOYSA-N 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 238000002559 palpation Methods 0.000 description 1
- 235000011837 pasties Nutrition 0.000 description 1
- 230000037361 pathway Effects 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 125000002467 phosphate group Chemical group [H]OP(=O)(O[H])O[*] 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 239000003495 polar organic solvent Substances 0.000 description 1
- 229920001983 poloxamer Polymers 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 239000001205 polyphosphate Substances 0.000 description 1
- 235000011176 polyphosphates Nutrition 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920000166 polytrimethylene carbonate Polymers 0.000 description 1
- 239000001103 potassium chloride Substances 0.000 description 1
- 235000011164 potassium chloride Nutrition 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 239000013615 primer Substances 0.000 description 1
- 239000002987 primer (paints) Substances 0.000 description 1
- CTPKUPQTROHREC-UHFFFAOYSA-N prop-2-enyl 3-chloropropanoate Chemical compound ClCCC(=O)OCC=C CTPKUPQTROHREC-UHFFFAOYSA-N 0.000 description 1
- YVAMVRSKOCSBPY-UHFFFAOYSA-N prop-2-ynyl 2-chloroacetate Chemical compound ClCC(=O)OCC#C YVAMVRSKOCSBPY-UHFFFAOYSA-N 0.000 description 1
- YDELXAFUTFIRRH-UHFFFAOYSA-N prop-2-ynyl 3-chloropropanoate Chemical compound ClCCC(=O)OCC#C YDELXAFUTFIRRH-UHFFFAOYSA-N 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 230000005588 protonation Effects 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 206010037844 rash Diseases 0.000 description 1
- 239000002964 rayon Substances 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 235000003441 saturated fatty acids Nutrition 0.000 description 1
- 150000003333 secondary alcohols Chemical class 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 235000017550 sodium carbonate Nutrition 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- FVEFRICMTUKAML-UHFFFAOYSA-M sodium tetradecyl sulfate Chemical compound [Na+].CCCCC(CC)CCC(CC(C)C)OS([O-])(=O)=O FVEFRICMTUKAML-UHFFFAOYSA-M 0.000 description 1
- 239000011122 softwood Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 125000004434 sulfur atom Chemical group 0.000 description 1
- 239000000271 synthetic detergent Substances 0.000 description 1
- 239000004758 synthetic textile Substances 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 238000009988 textile finishing Methods 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 125000004001 thioalkyl group Chemical group 0.000 description 1
- 125000003396 thiol group Chemical group [H]S* 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 238000010023 transfer printing Methods 0.000 description 1
- 125000004665 trialkylsilyl group Chemical group 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- 125000000725 trifluoropropyl group Chemical group [H]C([H])(*)C([H])([H])C(F)(F)F 0.000 description 1
- 229940057400 trihydroxystearin Drugs 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- UHVMMEOXYDMDKI-JKYCWFKZSA-L zinc;1-(5-cyanopyridin-2-yl)-3-[(1s,2s)-2-(6-fluoro-2-hydroxy-3-propanoylphenyl)cyclopropyl]urea;diacetate Chemical compound [Zn+2].CC([O-])=O.CC([O-])=O.CCC(=O)C1=CC=C(F)C([C@H]2[C@H](C2)NC(=O)NC=2N=CC(=CC=2)C#N)=C1O UHVMMEOXYDMDKI-JKYCWFKZSA-L 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
- C08L83/04—Polysiloxanes
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/42—Block-or graft-polymers containing polysiloxane sequences
- C08G77/46—Block-or graft-polymers containing polysiloxane sequences containing polyether sequences
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/48—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule in which at least two but not all the silicon atoms are connected by linkages other than oxygen atoms
- C08G77/54—Nitrogen-containing linkages
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/643—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain
- D06M15/6436—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain containing amino groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/02—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Silicon Polymers (AREA)
- Paper (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Cosmetics (AREA)
- Paints Or Removers (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10321558 | 2003-05-14 | ||
| DE10321558.1 | 2003-05-14 | ||
| PCT/EP2004/050797 WO2004101684A1 (de) | 2003-05-14 | 2004-05-13 | Polyorganosiloxan-zusammensetzungen zur behandlung von substraten |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2007504344A JP2007504344A (ja) | 2007-03-01 |
| JP4936893B2 true JP4936893B2 (ja) | 2012-05-23 |
Family
ID=33440777
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2006530191A Expired - Fee Related JP4936893B2 (ja) | 2003-05-14 | 2004-05-13 | 基質処理用ポリオルガノシロキサン組成物 |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US7897716B2 (ko) |
| EP (1) | EP1625180B1 (ko) |
| JP (1) | JP4936893B2 (ko) |
| KR (1) | KR101002901B1 (ko) |
| CN (1) | CN100384940C (ko) |
| AT (1) | ATE340224T1 (ko) |
| BR (1) | BRPI0410310B1 (ko) |
| CA (1) | CA2540317A1 (ko) |
| DE (1) | DE502004001543D1 (ko) |
| MX (1) | MXPA05012221A (ko) |
| WO (1) | WO2004101684A1 (ko) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7479578B2 (en) * | 2003-12-19 | 2009-01-20 | Kimberly-Clark Worldwide, Inc. | Highly wettable—highly flexible fluff fibers and disposable absorbent products made of those |
| US7811948B2 (en) | 2003-12-19 | 2010-10-12 | Kimberly-Clark Worldwide, Inc. | Tissue sheets containing multiple polysiloxanes and having regions of varying hydrophobicity |
| DE102005014312A1 (de) * | 2005-03-30 | 2006-10-19 | Ge Bayer Silicones Gmbh & Co. Kg | Zusammensetzung enhaltend Polyamino- und/oder Polyammonium-Polysiloxan-Verbindungen auf einem Substrat |
| DE102005036602A1 (de) * | 2005-08-01 | 2007-02-08 | Ge Bayer Silicones Gmbh & Co. Kg | Polyammonium-Polysiloxancopolymere |
| CA2637772A1 (en) * | 2006-02-09 | 2007-08-16 | Basf Se | Method for treating polypropylene textiles |
| WO2008138363A1 (de) * | 2007-05-10 | 2008-11-20 | Evonik Goldschmidt Gmbh | Stickstoffhaltige polyether-polysiloxan-blockcopolymere , verfahren zu deren herstellung und deren verwendung zur verbesserung der oberflächeneigenschaften von geweben und fasern |
| DE102007023869A1 (de) * | 2007-05-21 | 2008-12-18 | Momentive Performance Materials Gmbh & Co. Kg | Neue Polycarbonat- und/oder Polyurethan-Polyorganosiloxan-Verbindungen |
| DE102007037345A1 (de) * | 2007-08-08 | 2009-02-12 | Wacker Chemie Ag | Quaternäre Ammoniumgruppen aufweisende Organosiliciumverbindungen und deren Herstellung |
| DE102008014761A1 (de) * | 2008-03-18 | 2009-12-10 | Momentive Performance Materials Gmbh | Verwendung von Polyamino- und/oder Polyammonium-Polysiloxan-Copolymer-Verbindungen |
| JP6046505B2 (ja) * | 2013-01-29 | 2016-12-14 | 株式会社ダイセル | シート状モールド及びその製造方法並びにその用途 |
| CN116018367A (zh) | 2020-09-09 | 2023-04-25 | 瓦克化学股份公司 | 低环化衍生的氨基官能化硅氧烷聚合物在处理纤维基质中的用途 |
Citations (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH05209058A (ja) * | 1991-09-13 | 1993-08-20 | General Electric Co <Ge> | アミノ官能性シリコーンミクロエマルジョンの製造法 |
| JPH06311943A (ja) * | 1993-04-28 | 1994-11-08 | Toray Dow Corning Silicone Co Ltd | 拭き取り紙処理用シリコーンエマルジョン組成物 |
| JPH11158779A (ja) * | 1997-11-25 | 1999-06-15 | Toshiba Silicone Co Ltd | 繊維処理剤 |
| JP2001513534A (ja) * | 1997-08-25 | 2001-09-04 | ロレアル | アミンポリオキシアルキレンシリコーンブロックとコンディショニング剤を含有する化粧品用組成物とその用途 |
| WO2002010257A1 (de) * | 2000-07-27 | 2002-02-07 | Ge Bayer Silicones Gmbh & Co. Kg | Polyammonium-polysiloxan-verbindungen, verfahren zu ihrer herstellung und ihre verwendung |
| WO2002066559A1 (en) * | 2001-02-20 | 2002-08-29 | Crompton Corporation | Organopolysiloxane composition, method of making emulsion-forming organopolysiloxane composition and method of treating textile fiber or fabric |
| JP2003073477A (ja) * | 2001-08-14 | 2003-03-12 | Wacker Chemie Gmbh | 四級アンモニウム基を有しているオルガノポリシロキサン及びその製造方法 |
| JP2004331977A (ja) * | 2003-05-08 | 2004-11-25 | Wacker Chemie Gmbh | ポリアルコキシ基を有する有機ケイ素化合物およびその製法 |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5098979A (en) * | 1991-03-25 | 1992-03-24 | Siltech Inc. | Novel silicone quaternary compounds |
| US5707435A (en) | 1996-10-16 | 1998-01-13 | Dow Corning Corporation | Ammonium siloxane emulsions and their use as fiber treatment agents |
| US5707434A (en) | 1996-10-16 | 1998-01-13 | Dow Corning Corporation | Water soluble ammonium siloxane compositions and their use as fiber treatment agents |
| FR2802540B1 (fr) * | 1999-12-17 | 2002-05-24 | Rhodia Chimie Sa | Procede de preparation de polyorganosiloxanes par polymerisation catalysee par un systeme catalytique a base d'acide triflique ou de derives de l'acide triflique |
| US7041767B2 (en) | 2000-07-27 | 2006-05-09 | Ge Bayer Silicones Gmbh & Co. Kg | Polysiloxane polymers, method for their production and the use thereof |
| WO2002010256A1 (de) * | 2000-07-27 | 2002-02-07 | Ge Bayer Silicones Gmbh & Co. Kg | Ein- oder mehrfachquartäre polysiloxane |
| US6903061B2 (en) * | 2000-08-28 | 2005-06-07 | The Procter & Gamble Company | Fabric care and perfume compositions and systems comprising cationic silicones and methods employing same |
| US6818610B2 (en) * | 2001-07-27 | 2004-11-16 | Procter & Gamble Company | Fabric care systems for providing anti-wrinkle benefits to fabric |
-
2004
- 2004-05-13 US US10/556,124 patent/US7897716B2/en not_active Expired - Fee Related
- 2004-05-13 WO PCT/EP2004/050797 patent/WO2004101684A1/de active IP Right Grant
- 2004-05-13 EP EP04741569A patent/EP1625180B1/de not_active Expired - Lifetime
- 2004-05-13 MX MXPA05012221A patent/MXPA05012221A/es active IP Right Grant
- 2004-05-13 AT AT04741569T patent/ATE340224T1/de not_active IP Right Cessation
- 2004-05-13 DE DE502004001543T patent/DE502004001543D1/de not_active Expired - Lifetime
- 2004-05-13 CA CA002540317A patent/CA2540317A1/en not_active Abandoned
- 2004-05-13 JP JP2006530191A patent/JP4936893B2/ja not_active Expired - Fee Related
- 2004-05-13 CN CNB2004800204200A patent/CN100384940C/zh not_active Expired - Fee Related
- 2004-05-13 KR KR1020057021608A patent/KR101002901B1/ko active IP Right Grant
- 2004-05-13 BR BRPI0410310-6A patent/BRPI0410310B1/pt not_active IP Right Cessation
Patent Citations (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH05209058A (ja) * | 1991-09-13 | 1993-08-20 | General Electric Co <Ge> | アミノ官能性シリコーンミクロエマルジョンの製造法 |
| JPH06311943A (ja) * | 1993-04-28 | 1994-11-08 | Toray Dow Corning Silicone Co Ltd | 拭き取り紙処理用シリコーンエマルジョン組成物 |
| JP2001513534A (ja) * | 1997-08-25 | 2001-09-04 | ロレアル | アミンポリオキシアルキレンシリコーンブロックとコンディショニング剤を含有する化粧品用組成物とその用途 |
| JPH11158779A (ja) * | 1997-11-25 | 1999-06-15 | Toshiba Silicone Co Ltd | 繊維処理剤 |
| WO2002010257A1 (de) * | 2000-07-27 | 2002-02-07 | Ge Bayer Silicones Gmbh & Co. Kg | Polyammonium-polysiloxan-verbindungen, verfahren zu ihrer herstellung und ihre verwendung |
| WO2002066559A1 (en) * | 2001-02-20 | 2002-08-29 | Crompton Corporation | Organopolysiloxane composition, method of making emulsion-forming organopolysiloxane composition and method of treating textile fiber or fabric |
| JP2003073477A (ja) * | 2001-08-14 | 2003-03-12 | Wacker Chemie Gmbh | 四級アンモニウム基を有しているオルガノポリシロキサン及びその製造方法 |
| JP2004331977A (ja) * | 2003-05-08 | 2004-11-25 | Wacker Chemie Gmbh | ポリアルコキシ基を有する有機ケイ素化合物およびその製法 |
Also Published As
| Publication number | Publication date |
|---|---|
| KR20060011867A (ko) | 2006-02-03 |
| DE502004001543D1 (de) | 2006-11-02 |
| CN1823135A (zh) | 2006-08-23 |
| WO2004101684A1 (de) | 2004-11-25 |
| BRPI0410310A (pt) | 2006-05-23 |
| ATE340224T1 (de) | 2006-10-15 |
| MXPA05012221A (es) | 2006-02-10 |
| BRPI0410310B1 (pt) | 2014-02-18 |
| EP1625180B1 (de) | 2006-09-20 |
| EP1625180A1 (de) | 2006-02-15 |
| CN100384940C (zh) | 2008-04-30 |
| US20060237155A1 (en) | 2006-10-26 |
| US7897716B2 (en) | 2011-03-01 |
| CA2540317A1 (en) | 2004-11-25 |
| KR101002901B1 (ko) | 2010-12-21 |
| JP2007504344A (ja) | 2007-03-01 |
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